1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111328 | juvenile myoclonic epilepsy 9 | A juvenile myoclonic epilepsy that has_material_basis_in heterozygous variation in a region on chromosome 2q33-q36. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |
